Canonical Allele Identifier: CA325522001

Gene: MIOX

Linked Data

• dbSNP Id: rs113284967
• MyVariant Identifiers: chr22:g.50928352C>G (hg19) ; chr22:g.50489923C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50489923C>G , CM000684.2:g.50489923C>G	GRCh38
NC_000022.10:g.50928352C>G , CM000684.1:g.50928352C>G	GRCh37
NC_000022.9:g.49275218C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000216075.11:c.*67C>G MANE Select	ENSP00000216075.6:n.*67C>G
ENST00000216075.10:c.*67C>G	ENSP00000216075.6:n.*67C>G
ENST00000395732.7:c.*98C>G	ENSP00000379081.3:n.*98C>G
ENST00000395733.7:c.*98C>G	ENSP00000379082.3:n.*98C>G
ENST00000451761.1:c.865C>G	ENSP00000409894.1:n.865C>G
NM_017584.5:c.*67C>G	NP_060054.4:n.*67C>G
XM_005261925.3:c.*67C>G	XP_005261982.1:n.*67C>G
XR_244455.2:n.3421C>G
XM_005261925.4:c.*67C>G	XP_005261982.1:n.*67C>G
NM_017584.6:c.*67C>G MANE Select	NP_060054.4:n.*67C>G